WO1986002832A1 - Effervescent compositions - Google Patents
Effervescent compositions Download PDFInfo
- Publication number
- WO1986002832A1 WO1986002832A1 PCT/US1985/002249 US8502249W WO8602832A1 WO 1986002832 A1 WO1986002832 A1 WO 1986002832A1 US 8502249 W US8502249 W US 8502249W WO 8602832 A1 WO8602832 A1 WO 8602832A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- effervescent
- zeolite
- gas
- inorganic oxide
- oxide material
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/128—Aluminium silicates, e.g. zeolites
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/26—Aluminium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0052—Gas evolving or heat producing compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/22—Gas releasing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/22—Gas releasing
- A61K2800/222—Effervescent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/56—Compounds, absorbed onto or entrapped into a solid carrier, e.g. encapsulated perfumes, inclusion compounds, sustained release forms
Definitions
- the invention relates to the field of effervescent compositions and to the process for providing an effervescent action by employing a gas-containing inorganic oxide material in an essentially anhydrous base medium.
- a method for providing an effervescent mouthwash is disclosed in U.S. Patent No. 3,947,567 wherein a liquified gas is distributed under pressure in an aerosol dispensing container. The release of the pressurized mouthwash results in release of the liquified gas.
- Effervescent compositions that provide an effervescent/mechanical-cleaning action during use.
- the effervescent compositions comprise an essentially anhydrous base medium and an inorganic oxide material containing up to about 25 percent by weight of an adsorbed gas, e.g., carbon dioxide.
- the effervescent compositions also provide an astringent sensation when contacted with the skin as a result of the effervescent cleaning action and when carbon dioxide is the adsorbed gas by the in situ generation of carbonic acid.
- the invention relates to essentially anhydrous compositions which provide an effervescent action and mechanical cleansing action when contacted with water.
- This effervescent action is both stimulating when in contact with human skin and provides a mechanical mixing action which enhances cleaning and effective distribution of active components present in the effervescent composition.
- the effervescent compositions are formed from an essentially anhydrous base medium and a gas-containing inorganic oxide material.
- the effervescent compositions of the instant invention are unique in their providing an effervescent action without the need of chemical acid/base reactions.
- the effervescent compositions are formed by use of an inorganic oxide material, e.g., icroporous molecular sieves, having sufficient adsorbed gas such that when contained in an essentially anhydrous composition that is contacted with water that a release of the adsorbed gas occurs to provide an effervescent effect.
- the inorganic oxide material preferably a microporous inorganic oxide material, employed in the effervescent compositions are usually at least partially dehydrated, i.e., such materials have had at least a portion of their chemically reactive water removed by thermal or chemical treatment.
- Such materials may be prepared by calcination of the hydrated materials at temperatures above 100°C in air or other gas. Dehydration of the inorganic oxide material may be carried out at temperatures below 100°C when subat ospheric pressures are employed.
- the dehydrated inorganic oxide materials preferably contain less than about 5 percent by weight water, and more preferably less than about 3 percent by weight.
- the effervescent compositions of the instant invention comprise an essentially anhydrous base medium and a gas-containing inorganic oxide material.
- the gas may be any gas capable of being adsorbed by the inorganic oxide material in sufficient effective amount to provide effervescent action upon contacting of the effervescent composition with water.
- the adsorbed gas is generally present in an amount between about 1 and 25 weight percent of the total weight of the adsorbed gas and inorganic oxide material. Since the effervescent action of the desorbing gas provides a mechanical cleaning and mixing action, it is preferred to have between about 10 and 25 weight percent of the adsorbed gas present.
- the inorganic oxide material may be any material capable of adsorbing an effective amount of a gas which upon contact with water desorbs the gas in favor of the adsorption of water.
- the inorganic oxide material can be any of the zeolitic alu inosilicates capable of adsorbing an effective amount of a gas, an aluminophosphate, e.g., as disclosed in U.S. Patent No. 4,310,440, a silicoaluminophosphate, e.g., as disclosed in U.S. Patent No. 4,440,871, aluminas, silicas, silica-aluminas and the like.
- the inorganic oxide material is preferably a microporous material since microporous materials demonstrate gas adsorption characteristics as a result of the pore structure of the material.
- microporous materials demonstrate gas adsorption characteristics as a result of the pore structure of the material.
- Such materials are silicalite, zeolite A, zeolite B, zeolite X, zeolite Y, zeolite P, zeolite , zeolite L, zeolite F, ZSM-type zeolites, natural zeolites such as analcite, chabazite, clinoptilolite, errionite, pawlingite, priolite, ferrierite, mordenite, levynite, etc., and mixtures thereof.
- the zeolite may contain cations of alkali metals, alkaline earth metals, zinc, copper, etc., or any other suitable cation.
- the gas-containing inorganic oxide material may be present in the effervescent composition in an effective amount up to about 99 percent of weight (wt.-t) of the total weight of the effervescent composition and such is typically the case when a powdered effervescent composition is desired.
- the effervescent compositions preferably contain between about 1 wt.-t and about 60 wt.t and more preferably between about 5 wt.t and about 50 wtt of the gas-containing inorganic oxide material.
- the gas-containing inorganic oxide material may also act as an abrasive.
- the particle size of the gas-containing inorganic oxide material is preferably less than 10 microns and preferably has a particle size distribution with less than 10 percent, more preferably less than 5 percent by weight of the particles having a mean particle diameter greater than 5 microns.
- the gas to be employed on this instant invention may be any gas which is a gas at 18°C and above and which when adsorbed by the inorganic oxide material will then desorb upon being contacted with water.
- the gas may be, but is not limited to, nitrogen, oxygen, helium, argon, carbon dioxide, fluorine, chlorine and the like and mixtures thereof.
- the preferred gas for compositions which contact the skin is carbon dioxide owing to its ability to form carbonic acid when it contacts water and thus provide an astringent effect.
- the preferred gas-containing inorganic oxide material is a carbon dioxide-containing inorganic oxide material formed by contacting an at least partially dehydrated material with carbon dioxide under effective conditions that result in the adsorption of carbon dioxide by the inorganic oxide material.
- the inorganic oxide material will adsorb between about 1 and about 25 percent by weight carbon dioxide, based on the weight of said carbon dioxide and inorganic oxide material.
- the inorganic oxide material preferably adsorbs between about 5 and about 20 percent by weight carbon dioxide.
- the preferred zeolites are zeolite A, zeolite B, zeolite X, zeolite Y, zeolite P, chabazite and mordenite.
- the effervescent compositions are formed with an essentially anhydrous base medium as heretofore employed in the formulations of anhydrous compositions.
- the term "essentially anhydrous” is meant to denote a composition, i.e., base-medium that has a water content sufficiently low so as not to cause the adsorbed gas to be desorbed from the inorganic oxide material prior to contact with water.
- U.S. Patent No. 3,250,680 incorporated herein by reference thereto, discloses a number of such anhydrous media for hand cleansers, cleansing creams, ' hand lotions, toothpaste, beauty masks, all-purpose creams, liquifying cleansing creams, ointments and cream shampoo. Powdered effervescent compositions may also be formed.
- the essentially anhydrous base medium can include flavor components, coloring agents, polishing agents, thickeners, organic surface-active agents and the like.
- gas-containing inorganic oxide materials may be employed in essentially anhydrous base media of the type generally employed for preparing detergents, powdered cleansers, liquid cleansers, polishing compositions, toilet bowl cleansers, carpet cleaning compositions, stain removing compositions, oven cleaning compositions and the like.
- essentially anhydrous detergent compositions may be prepared according to the disclosure of U.S. Patent No. 4,333,771, incorporated herein by reference thereto, by employing an effective amount of a gas-containing inorganic oxide in accordance with the instant invention. The formulation of such compositions are well known in the art.
- Suitable flavoring or sweetening agents or mixture thereof, if any, may be employed in formulating a flavor for the effervescent compositions of the present invention.
- suitable flavoring constituents include the flavoring oils, e.g. oils of spearmint, peppermint, wintergreen, sassafras, clove, sage, eucalyptus, marjoram, cinnamon, lemon, lime, grapefruit and orange as well as flavoring aldehydes, esters such as methyl salicylate, alcohols, and higher fatty compounds known in the art. Also useful are such chemicals as menthol, carvone and anethole.
- oils of peppermint, spearmint, and eucalyptus are the oils of peppermint, spearmint, and eucalyptus, and anethole, menthol and carvone.
- flavorful solvents such as chloroform and mock chloroform, may be employed.
- Such flavorings may be used as liquids or may be solidified by being mixed with a particulate carrier material, such as starch, calcium carbonate, paraffin, vegetable wax, fat, higher fatty acid o ⁇ other suitable carrier substances.
- the flavor ⁇ ay be converted to liquid form, if so desired, by dissolving it in the solvent or emulsifying it, usually with the help of asynthetic or natural emulsifying agent.
- the choice as to whether to utilize particulate solid or liquid flavors or to convert such flavors to a particulate solid or liquid form, respectively, will often depend on the properties desired in the flavor and its compatibility with the sweetener and any other material to be present with it.
- Suitable sweetening agents include mannitol, sucrose, lactose, maltose, sorbitol, xylitol, sodium cyclamate, saccharin, the dipeptides of the U.S. Pat. No. 3,939,261 and the oxathiazin salts of U.S. Pat. No. 3,932,606.
- flavor and sweetening agent may together comprise from about 0.1 to 10* or more of the compositions of the instant invention.
- the effervescent compositions of this invention may also include additional polishing agents of the type commonly employed heretofore as abrasives.
- Such polishing agents are usually finely divided water insoluble powdered materials. They are generally from 1 to 40 microns, most preferably from 2 to 20 microns in particle sizes, with distribution of normal particle sizes being over the range.
- Representative polishing agents include, for example, dicalcium phosphate, tricalcium phosphate, insoluble sodium metaphosphate, aluminum hydroxide, colloidal silica, SYLOID 74 (a micron sized synthetic silica) magnesium carbonate, calcium carbonate, calcium prophosphate, bentonite, amorphous alumino-silicate, etc., including suitable mixtures thereof.
- Such additional polishing agents may be present in an amount up to a maximum of 20% by weight of the formulation and are preferably present in an amount no more than 101, the amount depending on the desired abrasivity and characteristics of the effervescent composition.
- the effervescent compositions of this invention include liquids and solids that maybe proportioned to form a creamy mass of desired consistency which is extrudable from an aerosol or other pressurized container or a collapsible tube (for example aluminum).
- the liquids in a cream formulation will comprise chiefly glycerine or an oil, propylene glycol, polyethylene glycol 400, etc., including suitable mixtures thereof.
- the total liquid content will generally be about 20 to 75 percent by weight of the effervescent composition.
- a gelling agent in cream formulations and gels may be employed, such as the natural and synthetic gums and gum-like materials, for example, Irish moss, gum tragacanth, methyl cellulose, polyvinylpyrroliaone, hydrophilic colloidal carboxyvinyl polymers such as those sold under the trademark Carbopol 934 and 940, hydroxyethyl cellulose, Indian gum, acacia gums, agar agar, locust bean gum, synthetic silicated clays such as those sold under the trademark Laponite CP and Laponite SP, pectin and finely divided pyrogenic silica, sold under the trademarks Cab-0-Sil M5, Syloid 244, Syloid 266 and Aerosol D 200.
- the natural and synthetic gums and gum-like materials for example, Irish moss, gum tragacanth, methyl cellulose, polyvinylpyrroliaone, hydrophilic colloidal carboxyvinyl polymers such as those sold under the trademark Carbopol 934 and
- the proportions of gelling agents or thickeners in extrudable effervescent compositions are sufficient to form an extrudable, shape-retaining product which can be squeezed from a tube and substantially maintain its shape thereon. In most cases no more than about 101 of gelling agent need be used and in most instances about 0.5 to 10t will suffice, and preferably about 1 to 5-t.
- Suitable oils for use in form effervescent compositions include those which have viscosities ranging from about 100 to about 300 centipoises at 70°F. Oils employable herein include mineral oil, light liquid petrolatum thickened to the necessary viscosity; and vegetable oils.
- a mineral oil commonly employed in cosmetic compositions is Mineral Oil U.S.P. also known as Liquid Petrolatum U.S.P., mineral oil (heavy medicinal) white mineral oil, liquid paraffin, and heavy liquid petrolatum.
- Mineral oil U.S.P. is defined in-Remingt ⁇ n's Pharmaceutical Sciences, 13th edition, Mack Publishing Co., Easton, Pa. 1965 as "a mixture of liquid hydrocarbons obtained from petroleum; a colorless transparent, oily liquid, free or nearly free from fluoroescene". It is tasteless and odorless when cold and develops not more than a faint odor of petroleum when heated.
- a light liquid petrolatum employable herein is Light Liquid Petrolatum N.F. also known as light liquid paraffin and light white mineral oil It is described in Remington's Pharmaceutical Sciences, as "... a mixture of liquid hydrocarbons obtained from petroleum, it may contain a stabilizer". If Light Liquid Petrolatum N.F. is used as the oil it may be thickened to the desired viscosity of -from about 100 to about 300 centipoises at 70 # F with one of the well-known commercially available inert thickening materials, such as a pyrogenic silica sold under the trademark Cab-0-Sil, or a hydrogenated castor oil, sold under the tradename THIXIN.
- a pyrogenic silica sold under the trademark Cab-0-Sil
- a hydrogenated castor oil sold under the tradename THIXIN.
- Suitable vegetable oils which may be used as the oil ingredient include coconut oil, cotton-seed oil, sesame oil and similar non-toxic vegetable oils, as described in Vegetable Fats and Oils by E. W. Eckey, Reinhold Publishing Corp., New York, 1954.
- the vegetable oil is desirably selected to fall within the viscosity range of from about 100 t about 300 centipoises. A particular vegetable oil falling within this range is NEOBFE M-5, a fractional triglyceride of coconut oil.
- the vegetable oil ingredient may contain a minor amount of an anti-oxidant such as butylated gydroxyanisole or butylated hydroxytoluene, preferably in an amount ranging from about 0.1 to about 3-t by weight, based on the weight of the vegetable oil employed.
- an anti-oxidant such as butylated gydroxyanisole or butylated hydroxytoluene
- the liquid vehicle of an extrudable effervescent composition together with the gelling agent(s) and other constituents, will form an extrudable mass of a non-dripping consistency when extruded from a collapsible tube, such as an aluminum tube.
- a collapsible tube such as an aluminum tube.
- the effervescent composition can be thinned and conversely, by the addition of more solids, especially more gelling agents and/or the gas-containing material, the effervescent compositions can be thickened.
- the liquid portion comprises glycerine.
- glycerine it is preferred to employ glycerine, other suitable vehicles in place thereof or in addition thereto may also be present, either with the mentioned polyhydric alcohols or in replacement for them.
- propylene glycol, polyethylene glycol, and polypropylene glycol may be employed providing that they are physiologically acceptable and produce products having a desired refractive index, in the case of the manufacture of visually clear effervescent compositions.
- the use of glycerine in the liquid vehicle is particularly advantageous in acting with the zeolite component in effecting utilization of the flavor components of the effervescent compositions.
- the proportion of vehicle is determined by the physical properties of the extrudate. Usually, however, from about 10 to 901 of the vehicle will be employed, with about 10 to 35* being a typical range for the production of opaque formulations and about 40 to 90* being useful for the manufacture of clear formulations.
- the preferred liquid vehicle is an anhydrous humectant or oil selected from the group consisting of glycerine, propylene glycol, polyethylene glycol * , polypropylene glycol, liquid light petrolatum, mineral oil, vegetable oil and suitable mixtures thereof. - 13 -
- the gelling agents is desirably selected from the group consisting of sodium carboxymethyl cellulose, hydroxyethyl cellulose, polyvinyl alcohol, Irish moss, silica aerogel or mixtures thereof.
- the solids and liquids are proportioned similarly to the amounts above noted and the flavor is blended with the solids and liquids, and a waxy matrix such as polyethylene glycol having a molecular weight of about 6,000 by weight, generally in amounts of about 4-20 percent by weight, in order to facilitate the formation of a table of the desired size and shape.
- a waxy matrix such as polyethylene glycol having a molecular weight of about 6,000 by weight, generally in amounts of about 4-20 percent by weight, in order to facilitate the formation of a table of the desired size and shape.
- polishing agents and other listings of other components of the effervescent composition given in the present specifications are not intended to be exhaustive and therefore, for other materials of these types reference should be made to a standard handbook, such as Cosmetics: Science and Technology, by Saccharin, 2and printing, 1963, published by Interscience Publishers, Inc.
- Organic surface-active agents are generally employed in effervescent compositions to assist in achieving through and complete dispersion of the components of such compositions during use and render the instant compositions more cosmetically acceptable.
- the organic surface-active material may be anionic, nonionic, ampholytic, or cationic in nature, and it is preferred to employ a surface-active agent which imparts to the composition detersive and foaming properties.
- Such detergents are water-soluble salts of higher fatty acid monoglyceride monosulfates, such as the sodium salt of the monosulfated monoglyceride of hydrogenated coconut oil fatty acids, higher alkyl sulfates, such as sodium lauryl sulfate, alkyl aryl sulfonates.such as sodium dodecyl benzene sulfonate, higher alkyl sulfoacetates, higher fatty acid ester of 1.2-dihydroxy propane sulfonates, and the substantially saturated high aliphatic acyl amides of lower aliphatic amino carboxylic acid compounds, such as those having 12.to 16 carbon atoms in the fatty acid, or acyl radicals, and the like.
- higher fatty acid monoglyceride monosulfates such as the sodium salt of the monosulfated monoglyceride of hydrogenated coconut oil fatty acids
- higher alkyl sulfates such as sodium lauryl
- amides examples include N-lauroyl sarcosine, and the sodium potassium and ethanolamine salts of N-lauroyl, N-myristoyl, or N-palmitoyl sarcosine which should be substantially free from soap or similar higher fatty acid material which tends to substantially reduce the effect of these compounds.
- suitable surface-active materials include nonionic agents such as condensates of sorbitan monostearate with approximately 20 moles of ethylene oxide, condensates of ethylene oxide with propylene oxide, condensates of propylene glycol (“Pluronics”), and amphoteric agents such a quaternized imidazole derivatives which are available under the trademark "Miranol” such as Miranol C.M.
- suitable nonionic detergents are the condensation products of an alpha-olefin oxide containing 10 to 20 carbon atoms, a polyhydric alcohol containing 2 to 10 carbons and 2 to 6 hydroxyl groups and either ethylene oxide or a heteric mixture of ethylene oxide and propylene oxide.
- the resultant detergents are heteric polymers having a molecular weight in the range of 400 to about 1600 and containing 40* to 80* by weight of ethylene oxide, with an a-olefin oxide to polyhydric alcohol mole ratio in the range of about 1:1 to 1:3. These detergents are manufactured using well-known polymerization techniques under conditions of high temperature and high pressure. These nonionic detergents may be mixed with similar nonionic detergents as well as other types nonionic detergents described herein.
- olefin sulfonate detergents typically long chain alkenyl sulfonates.
- an effective amount of at least on surface-active material and generally between about 0.05 and 10* by weight and preferably between about 0.5 and 5* of at least one of the foregoing surface-active materials in the instant oral preparations.
- effervescent compositions of this invention Various other compatible and suitable materials may be incorporated in the effervescent compositions of this invention. Examples thereof are coloring or whitening agents or dyestuffs, preservatives, silicones, chlorophyll compounds, ammonated materials such as urea, diammonium phosphate and mixtures thereof, and other onstituents.
- coloring or whitening agents or dyestuffs preservatives
- silicones such as urea, diammonium phosphate and mixtures thereof, and other onstituents.
- chemical acid/base couples may be employed if additional in situ gas generation is desired, U.S. Patent No. 3,629,468 is respresentative of such acid/base couples.
- These adjuvants may be incorporated in the instant effervescent compositions in amounts which do not substantially adversely affect the properties and characteristics desired and are selected and used in proper amount depending upon the particular type of effervescent composition desired.
- Antibacterial agents may also be employed in the preparation of the instant effervescent compositions to provide a total content of such agents of up to about 10* by weight, preferably about 0.01 to 5.0* by weight, most preferably about 0.5 to 1.0* by weight, based on the total weight of the effervescent composition.
- the effervescent compositions may be prepared by suitably mixing the ingredients.
- a gelling agent such as silica aerogel or Carbopol 934 and a preservative such as dried benzoic acid, if employed, and sweetener, if used, is dispersed with a humectant such as glycerine.
- An abrasive agent including the gas-containing inorganic oxide material, surface-active agent and flavor may then separately added and uniformly dispersed.
- the paste is then thoroughly deareated (e.g., in vacuo) and
- Example 1 An carbon-dioxide containing zeolite was prepared using the sodium form of zeolite A.
- a sample of the zeolite As was placed in a cold air purged oven. The oven was heated to 480*C and maintained at this temperature for 2 hours to remove water from the zeolite. The oven and sample were then cooled to 300 ⁇ C.
- the dehydrated zeolite A was then placed in a container which had been purged with carbon dioxide for fifteen minutes prior to introduction of the dehydrated zeolite. The dehydrated zeolite remained in the container for 2 hours while carbon dioxide was introduced at a pressure of 16 psig. After two hours the container was sealed and the carbon dioxide-containing zeolite maintained under a carbon dioxide atmosphere. A portion of the carbon dioxide-containing zeolite A was analyzed and contained 13.37 percent by weight carbon dioxide, based on the weight of the zeolite.
- Example 2 Example 1 was repeated except that a Y zeolite was employed instead of zeolite A. A portion of the carbon dioxide-containing zeolite Y was analyzed and contained 15.35 percent by weight carbon dioxide, based on the weight of the zeolite.
- Example 3 An effervescent composition was prepared using the carbon dioxide-containing Y zeolite prepared in example 2. The effervescent composition was prepared by placing all of the components in a glove box having a nitrogen atmosphere. The preparation was carried out under a nitrogen atmosphere. A slurry was formed by mixing 21.90 grams of the anhydrous carbon dioxide-containing Y zeolite with 26.75 grams of propylene glycol. This slurry was mixed with 0.075 grams benzoic acid, 0.3 grams of a silica sold under the trademark SYLOID 44, 1.00 gram sodium lauryl sulfate, 0.35 grams peppermint oil and 0.75 grams hydroxyl propyl cellulose. The mixture was blended and placed in a desiccator with an aspirator attached thereto. A portion of the final essentially anhydrous composition was added to water and observed to form a foam as carbon dioxide was released from the carbon dioxide-containing Y zeolite.
- Example 4 Example 3 was repeated except that the carbon dioxide-containing zeolite A of example 1 was employed to form an essentially anhydrous composition. The composition was observed to form a foam upon addition to water as carbon dioxide was released from the carbon dioxide-containing zeolite A.
- Example 5 Example 4 was repeated except that the peppermint oil was replaced by a sweetner. The toothpaste was observed to foam on being contacted with water as carbon dioxide was released from the carbon dioxide-containing zeolite.
- Example 6 The effect temperature on the effervescent activity of the effervescent composition of example 4 was evaluated by evaluating the effervescent time for three samples (2 grams each) in 500 milliliters of water at 18*C, 32*C and 50*C. The three samples were observed and the time recorded at which effervescent began and ended. The results were as follows:
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Dermatology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
Abstract
Effervescent compositions having an effervescent and cleansing action. The effervescent compositions are formed from an essentially anhydrous base medium and an inorganic oxide material containing an adsorbed gas. Upon contact of the composition with water an effervescent action occurs as the gas is desorbed from the inorganic oxide material.
Description
EFFERVESCENT COMPOSITIONS
The invention relates to the field of effervescent compositions and to the process for providing an effervescent action by employing a gas-containing inorganic oxide material in an essentially anhydrous base medium.
The development and formulation of effervescent compositions has traditionally been effected by use of various I situ chemical reactions which form a gas to provide an effervescent action. This type of acid/base reaction system is disclosed in U.S. Patent Nos. 1,297,494, 1,262,888, 1,516,398, 2,985,562, 3,772,431, 3,888, 976, 3,936,385, 3,962,417, 4,127,645, 4,180,467, 4,406,708 and 4,436,720. The cleansing benefits derived from an effervescent action is well documented in the above patents.
A method for providing an effervescent mouthwash is disclosed in U.S. Patent No. 3,947,567 wherein a liquified gas is distributed under pressure in an aerosol dispensing container. The release of the pressurized mouthwash results in release of the liquified gas.
Although the aforementioned acid/base and liquified gas methods provide an effervescent action such have not been widely employed. The instant invention provides a novel way to provide effervescence to anhydrous compositions when such are contacted with water.
SUMMARY OF THE INVENTION
Effervescent compositions are disclosed that provide an effervescent/mechanical-cleaning action during use. The effervescent compositions comprise an essentially anhydrous base medium and an inorganic oxide material containing up to about 25 percent by weight of an adsorbed gas, e.g., carbon dioxide. The effervescent compositions also provide an astringent sensation when contacted with the skin as a result of the effervescent cleaning action and when carbon dioxide is the adsorbed gas by the in situ generation of carbonic acid.
DETAILED DESCRIPTION OF THE INVENTION
The invention relates to essentially anhydrous compositions which provide an effervescent action and mechanical cleansing action when contacted with water. This effervescent action is both stimulating when in contact with human skin and provides a mechanical mixing action which enhances cleaning and effective distribution of active components present in the effervescent composition. The effervescent compositions are formed from an essentially anhydrous base medium and a gas-containing inorganic oxide material.
The effervescent compositions of the instant invention are unique in their providing an effervescent action without the need of chemical acid/base reactions. The effervescent compositions are formed by use of an inorganic oxide material, e.g., icroporous molecular sieves, having sufficient adsorbed gas such that when contained in an essentially anhydrous composition that is
contacted with water that a release of the adsorbed gas occurs to provide an effervescent effect. The inorganic oxide material, preferably a microporous inorganic oxide material, employed in the effervescent compositions are usually at least partially dehydrated, i.e., such materials have had at least a portion of their chemically reactive water removed by thermal or chemical treatment. Such materials may be prepared by calcination of the hydrated materials at temperatures above 100°C in air or other gas. Dehydration of the inorganic oxide material may be carried out at temperatures below 100°C when subat ospheric pressures are employed. The dehydrated inorganic oxide materials preferably contain less than about 5 percent by weight water, and more preferably less than about 3 percent by weight.
The effervescent compositions of the instant invention comprise an essentially anhydrous base medium and a gas-containing inorganic oxide material. The gas may be any gas capable of being adsorbed by the inorganic oxide material in sufficient effective amount to provide effervescent action upon contacting of the effervescent composition with water. The adsorbed gas is generally present in an amount between about 1 and 25 weight percent of the total weight of the adsorbed gas and inorganic oxide material. Since the effervescent action of the desorbing gas provides a mechanical cleaning and mixing action, it is preferred to have between about 10 and 25 weight percent of the adsorbed gas present. Upon
contacting the essentially anhydrous effervescent composition with water the adsorbed gas will be released and an effervescent action occurs.
The inorganic oxide material may be any material capable of adsorbing an effective amount of a gas which upon contact with water desorbs the gas in favor of the adsorption of water. The inorganic oxide material can be any of the zeolitic alu inosilicates capable of adsorbing an effective amount of a gas, an aluminophosphate, e.g., as disclosed in U.S. Patent No. 4,310,440, a silicoaluminophosphate, e.g., as disclosed in U.S. Patent No. 4,440,871, aluminas, silicas, silica-aluminas and the like. The inorganic oxide material is preferably a microporous material since microporous materials demonstrate gas adsorption characteristics as a result of the pore structure of the material. Representative of such materials are silicalite, zeolite A, zeolite B, zeolite X, zeolite Y, zeolite P, zeolite , zeolite L, zeolite F, ZSM-type zeolites, natural zeolites such as analcite, chabazite, clinoptilolite, errionite, pawlingite, priolite, ferrierite, mordenite, levynite, etc., and mixtures thereof. A detailed discussion of such aluminosilicates and others is set forth in "ZEOLITE MOLECULAR SIEVES" by Donald . Breck, Wiley-Interscience Publication (1974). The zeolite may contain cations of alkali metals, alkaline earth metals, zinc, copper, etc., or any other suitable cation. The gas-containing inorganic oxide material may be present in the effervescent composition in an effective amount up to about 99 percent of weight
(wt.-t) of the total weight of the effervescent composition and such is typically the case when a powdered effervescent composition is desired. The effervescent compositions preferably contain between about 1 wt.-t and about 60 wt.t and more preferably between about 5 wt.t and about 50 wtt of the gas-containing inorganic oxide material. The gas-containing inorganic oxide material may also act as an abrasive. The particle size of the gas-containing inorganic oxide material is preferably less than 10 microns and preferably has a particle size distribution with less than 10 percent, more preferably less than 5 percent by weight of the particles having a mean particle diameter greater than 5 microns.
The gas to be employed on this instant invention may be any gas which is a gas at 18°C and above and which when adsorbed by the inorganic oxide material will then desorb upon being contacted with water. The gas may be, but is not limited to, nitrogen, oxygen, helium, argon, carbon dioxide, fluorine, chlorine and the like and mixtures thereof. The preferred gas for compositions which contact the skin is carbon dioxide owing to its ability to form carbonic acid when it contacts water and thus provide an astringent effect.
The preferred gas-containing inorganic oxide material is a carbon dioxide-containing inorganic oxide material formed by contacting an at least partially dehydrated material with carbon dioxide under effective conditions that result in the adsorption of carbon dioxide by the inorganic oxide material. The inorganic oxide material will adsorb between about 1 and about 25 percent by
weight carbon dioxide, based on the weight of said carbon dioxide and inorganic oxide material. The inorganic oxide material preferably adsorbs between about 5 and about 20 percent by weight carbon dioxide. The preferred zeolites are zeolite A, zeolite B, zeolite X, zeolite Y, zeolite P, chabazite and mordenite.
The effervescent compositions are formed with an essentially anhydrous base medium as heretofore employed in the formulations of anhydrous compositions. The term "essentially anhydrous" is meant to denote a composition, i.e., base-medium that has a water content sufficiently low so as not to cause the adsorbed gas to be desorbed from the inorganic oxide material prior to contact with water. U.S. Patent No. 3,250,680, incorporated herein by reference thereto, discloses a number of such anhydrous media for hand cleansers, cleansing creams,' hand lotions, toothpaste, beauty masks, all-purpose creams, liquifying cleansing creams, ointments and cream shampoo. Powdered effervescent compositions may also be formed. The essentially anhydrous base medium can include flavor components, coloring agents, polishing agents, thickeners, organic surface-active agents and the like.
In addition to the above, the gas-containing inorganic oxide materials may be employed in essentially anhydrous base media of the type generally employed for preparing detergents, powdered cleansers, liquid cleansers, polishing compositions, toilet bowl cleansers, carpet cleaning compositions, stain removing compositions, oven
cleaning compositions and the like. For example, essentially anhydrous detergent compositions may be prepared according to the disclosure of U.S. Patent No. 4,333,771, incorporated herein by reference thereto, by employing an effective amount of a gas-containing inorganic oxide in accordance with the instant invention. The formulation of such compositions are well known in the art.
Suitable flavoring or sweetening agents or mixture thereof, if any, may be employed in formulating a flavor for the effervescent compositions of the present invention. Examples of suitable flavoring constituents include the flavoring oils, e.g. oils of spearmint, peppermint, wintergreen, sassafras, clove, sage, eucalyptus, marjoram, cinnamon, lemon, lime, grapefruit and orange as well as flavoring aldehydes, esters such as methyl salicylate, alcohols, and higher fatty compounds known in the art. Also useful are such chemicals as menthol, carvone and anethole. Of these, the most commonly employed are the oils of peppermint, spearmint, and eucalyptus, and anethole, menthol and carvone. In some cases flavorful solvents, such as chloroform and mock chloroform, may be employed. Such flavorings may be used as liquids or may be solidified by being mixed with a particulate carrier material, such as starch, calcium carbonate, paraffin, vegetable wax, fat, higher fatty acid oτ other suitable carrier substances. In the cases of solid flavors, such as vanillin, sage, citric acid or licorice, the flavor ■ay be converted to liquid form, if so desired, by
dissolving it in the solvent or emulsifying it, usually with the help of asynthetic or natural emulsifying agent. The choice as to whether to utilize particulate solid or liquid flavors or to convert such flavors to a particulate solid or liquid form, respectively, will often depend on the properties desired in the flavor and its compatibility with the sweetener and any other material to be present with it. Suitable sweetening agents include mannitol, sucrose, lactose, maltose, sorbitol, xylitol, sodium cyclamate, saccharin, the dipeptides of the U.S. Pat. No. 3,939,261 and the oxathiazin salts of U.S. Pat. No. 3,932,606. Suitably, flavor and sweetening agent may together comprise from about 0.1 to 10* or more of the compositions of the instant invention.
The effervescent compositions of this invention may also include additional polishing agents of the type commonly employed heretofore as abrasives. Such polishing agents are usually finely divided water insoluble powdered materials. They are generally from 1 to 40 microns, most preferably from 2 to 20 microns in particle sizes, with distribution of normal particle sizes being over the range. Representative polishing agents include, for example, dicalcium phosphate, tricalcium phosphate, insoluble sodium metaphosphate, aluminum hydroxide, colloidal silica, SYLOID 74 (a micron sized synthetic silica) magnesium carbonate, calcium carbonate, calcium prophosphate, bentonite, amorphous alumino-silicate, etc., including suitable mixtures thereof. Such additional polishing agents
may be present in an amount up to a maximum of 20% by weight of the formulation and are preferably present in an amount no more than 101, the amount depending on the desired abrasivity and characteristics of the effervescent composition.
The effervescent compositions of this invention include liquids and solids that maybe proportioned to form a creamy mass of desired consistency which is extrudable from an aerosol or other pressurized container or a collapsible tube (for example aluminum). In general, the liquids in a cream formulation will comprise chiefly glycerine or an oil, propylene glycol, polyethylene glycol 400, etc., including suitable mixtures thereof. The total liquid content will generally be about 20 to 75 percent by weight of the effervescent composition. A gelling agent in cream formulations and gels may be employed, such as the natural and synthetic gums and gum-like materials, for example, Irish moss, gum tragacanth, methyl cellulose, polyvinylpyrroliaone, hydrophilic colloidal carboxyvinyl polymers such as those sold under the trademark Carbopol 934 and 940, hydroxyethyl cellulose, Indian gum, acacia gums, agar agar, locust bean gum, synthetic silicated clays such as those sold under the trademark Laponite CP and Laponite SP, pectin and finely divided pyrogenic silica, sold under the trademarks Cab-0-Sil M5, Syloid 244, Syloid 266 and Aerosol D 200.
The proportions of gelling agents or thickeners in extrudable effervescent compositions are sufficient to form an extrudable,
shape-retaining product which can be squeezed from a tube and substantially maintain its shape thereon. In most cases no more than about 101 of gelling agent need be used and in most instances about 0.5 to 10t will suffice, and preferably about 1 to 5-t.
Suitable oils for use in form effervescent compositions include those which have viscosities ranging from about 100 to about 300 centipoises at 70°F. Oils employable herein include mineral oil, light liquid petrolatum thickened to the necessary viscosity; and vegetable oils. A mineral oil commonly employed in cosmetic compositions is Mineral Oil U.S.P. also known as Liquid Petrolatum U.S.P., mineral oil (heavy medicinal) white mineral oil, liquid paraffin, and heavy liquid petrolatum. Mineral oil U.S.P. is defined in-Remingtόn's Pharmaceutical Sciences, 13th edition, Mack Publishing Co., Easton, Pa. 1965 as "a mixture of liquid hydrocarbons obtained from petroleum; a colorless transparent, oily liquid, free or nearly free from fluoroescene". It is tasteless and odorless when cold and develops not more than a faint odor of petroleum when heated.
A light liquid petrolatum employable herein is Light Liquid Petrolatum N.F. also known as light liquid paraffin and light white mineral oil It is described in Remington's Pharmaceutical Sciences, as "... a mixture of liquid hydrocarbons obtained from petroleum, it may contain a stabilizer". If Light Liquid Petrolatum N.F. is used as the oil it may be thickened to the desired viscosity of -from about 100 to about 300 centipoises at 70#F with one of the
well-known commercially available inert thickening materials, such as a pyrogenic silica sold under the trademark Cab-0-Sil, or a hydrogenated castor oil, sold under the tradename THIXIN.
Suitable vegetable oils which may be used as the oil ingredient include coconut oil, cotton-seed oil, sesame oil and similar non-toxic vegetable oils, as described in Vegetable Fats and Oils by E. W. Eckey, Reinhold Publishing Corp., New York, 1954. The vegetable oil is desirably selected to fall within the viscosity range of from about 100 t about 300 centipoises. A particular vegetable oil falling within this range is NEOBFE M-5, a fractional triglyceride of coconut oil. The vegetable oil ingredient may contain a minor amount of an anti-oxidant such as butylated gydroxyanisole or butylated hydroxytoluene, preferably in an amount ranging from about 0.1 to about 3-t by weight, based on the weight of the vegetable oil employed.
The liquid vehicle of an extrudable effervescent composition, together with the gelling agent(s) and other constituents, will form an extrudable mass of a non-dripping consistency when extruded from a collapsible tube, such as an aluminum tube. Thus, by the addition of more vehicle, the effervescent composition can be thinned and conversely, by the addition of more solids, especially more gelling agents and/or the gas-containing material, the effervescent compositions can be thickened. In typical effervescent compositions, the liquid portion comprises glycerine. Although it is preferred to
employ glycerine, other suitable vehicles in place thereof or in addition thereto may also be present, either with the mentioned polyhydric alcohols or in replacement for them. Thus, propylene glycol, polyethylene glycol, and polypropylene glycol may be employed providing that they are physiologically acceptable and produce products having a desired refractive index, in the case of the manufacture of visually clear effervescent compositions. The use of glycerine in the liquid vehicle is particularly advantageous in acting with the zeolite component in effecting utilization of the flavor components of the effervescent compositions. Normally the proportion of vehicle is determined by the physical properties of the extrudate. Usually, however, from about 10 to 901 of the vehicle will be employed, with about 10 to 35* being a typical range for the production of opaque formulations and about 40 to 90* being useful for the manufacture of clear formulations.
It is to be understood that while ordinarily where sorbitol or mannitol is employed in compositions, it is used as an aqueous solution, they may be employed herein, with the proviso, however, that it be substantially anhydrous.
The preferred liquid vehicle is an anhydrous humectant or oil selected from the group consisting of glycerine, propylene glycol, polyethylene glycol*, polypropylene glycol, liquid light petrolatum, mineral oil, vegetable oil and suitable mixtures thereof.
- 13 -
The gelling agents is desirably selected from the group consisting of sodium carboxymethyl cellulose, hydroxyethyl cellulose, polyvinyl alcohol, Irish moss, silica aerogel or mixtures thereof.
In the preparation of powdered effervescent compositions, it is usually sufficient to admix mechanically, e.g., by milling, the various solid ingredients, in appropriate quantities and particle sizes and thereafter carrying out procedures known in the art for packaging the product.
In chewable effervescent tablets the solids and liquids are proportioned similarly to the amounts above noted and the flavor is blended with the solids and liquids, and a waxy matrix such as polyethylene glycol having a molecular weight of about 6,000 by weight, generally in amounts of about 4-20 percent by weight, in order to facilitate the formation of a table of the desired size and shape.
The listing of polishing agents, and other listings of other components of the effervescent composition given in the present specifications are not intended to be exhaustive and therefore, for other materials of these types reference should be made to a standard handbook, such as Cosmetics: Science and Technology, by Saccharin, 2and printing, 1963, published by Interscience Publishers, Inc.
Organic surface-active agents are generally employed in effervescent compositions to assist in achieving through and complete dispersion of the components of such compositions during use and render the instant compositions more cosmetically
acceptable. The organic surface-active material may be anionic, nonionic, ampholytic, or cationic in nature, and it is preferred to employ a surface-active agent which imparts to the composition detersive and foaming properties. Suitably such detergents are water-soluble salts of higher fatty acid monoglyceride monosulfates, such as the sodium salt of the monosulfated monoglyceride of hydrogenated coconut oil fatty acids, higher alkyl sulfates, such as sodium lauryl sulfate, alkyl aryl sulfonates.such as sodium dodecyl benzene sulfonate, higher alkyl sulfoacetates, higher fatty acid ester of 1.2-dihydroxy propane sulfonates, and the substantially saturated high aliphatic acyl amides of lower aliphatic amino carboxylic acid compounds, such as those having 12.to 16 carbon atoms in the fatty acid, or acyl radicals, and the like. Examples of the last mentioned amides are N-lauroyl sarcosine, and the sodium potassium and ethanolamine salts of N-lauroyl, N-myristoyl, or N-palmitoyl sarcosine which should be substantially free from soap or similar higher fatty acid material which tends to substantially reduce the effect of these compounds.
Other suitable surface-active materials include nonionic agents such as condensates of sorbitan monostearate with approximately 20 moles of ethylene oxide, condensates of ethylene oxide with propylene oxide, condensates of propylene glycol ("Pluronics"), and amphoteric agents such a quaternized imidazole derivatives which are available under the trademark "Miranol" such as Miranol C.M.
Other suitable nonionic detergents are the condensation products of an alpha-olefin oxide containing 10 to 20 carbon atoms, a polyhydric alcohol containing 2 to 10 carbons and 2 to 6 hydroxyl groups and either ethylene oxide or a heteric mixture of ethylene oxide and propylene oxide. The resultant detergents are heteric polymers having a molecular weight in the range of 400 to about 1600 and containing 40* to 80* by weight of ethylene oxide, with an a-olefin oxide to polyhydric alcohol mole ratio in the range of about 1:1 to 1:3. These detergents are manufactured using well-known polymerization techniques under conditions of high temperature and high pressure. These nonionic detergents may be mixed with similar nonionic detergents as well as other types nonionic detergents described herein.
There may also be employed olefin sulfonate detergents, typically long chain alkenyl sulfonates.
It is typical to use an effective amount of at least on surface-active material and generally between about 0.05 and 10* by weight and preferably between about 0.5 and 5* of at least one of the foregoing surface-active materials in the instant oral preparations.
Various other compatible and suitable materials ma be incorporated in the effervescent compositions of this invention. Examples thereof are coloring or whitening agents or dyestuffs, preservatives, silicones, chlorophyll compounds, ammonated materials such as urea, diammonium phosphate and mixtures thereof, and other
onstituents. In addition, chemical acid/base couples may be employed if additional in situ gas generation is desired, U.S. Patent No. 3,629,468 is respresentative of such acid/base couples. These adjuvants may be incorporated in the instant effervescent compositions in amounts which do not substantially adversely affect the properties and characteristics desired and are selected and used in proper amount depending upon the particular type of effervescent composition desired.
Antibacterial agents may also be employed in the preparation of the instant effervescent compositions to provide a total content of such agents of up to about 10* by weight, preferably about 0.01 to 5.0* by weight, most preferably about 0.5 to 1.0* by weight, based on the total weight of the effervescent composition.
The effervescent compositions may be prepared by suitably mixing the ingredients. For instance in making a paste composition, a gelling agent such as silica aerogel or Carbopol 934 and a preservative such as dried benzoic acid, if employed, and sweetener, if used, is dispersed with a humectant such as glycerine. An abrasive agent, including the gas-containing inorganic oxide material, surface-active agent and flavor may then separately added and uniformly dispersed. The paste is then thoroughly deareated (e.g., in vacuo) and
» tubed.
Example 1 An carbon-dioxide containing zeolite was prepared using the sodium form of zeolite A. A sample of the zeolite As was placed in a cold air purged oven. The oven was heated to 480*C and maintained at this temperature for 2 hours to remove water from the zeolite. The oven and sample were then cooled to 300βC. The dehydrated zeolite A was then placed in a container which had been purged with carbon dioxide for fifteen minutes prior to introduction of the dehydrated zeolite. The dehydrated zeolite remained in the container for 2 hours while carbon dioxide was introduced at a pressure of 16 psig. After two hours the container was sealed and the carbon dioxide-containing zeolite maintained under a carbon dioxide atmosphere. A portion of the carbon dioxide-containing zeolite A was analyzed and contained 13.37 percent by weight carbon dioxide, based on the weight of the zeolite.
Example 2 Example 1 was repeated except that a Y zeolite was employed instead of zeolite A. A portion of the carbon dioxide-containing zeolite Y was analyzed and contained 15.35 percent by weight carbon dioxide, based on the weight of the zeolite.
Example 3 An effervescent composition was prepared using the carbon dioxide-containing Y zeolite prepared in example 2. The effervescent composition was prepared by placing all of the components in a glove box having a nitrogen atmosphere. The preparation was carried out under a nitrogen
atmosphere. A slurry was formed by mixing 21.90 grams of the anhydrous carbon dioxide-containing Y zeolite with 26.75 grams of propylene glycol. This slurry was mixed with 0.075 grams benzoic acid, 0.3 grams of a silica sold under the trademark SYLOID 44, 1.00 gram sodium lauryl sulfate, 0.35 grams peppermint oil and 0.75 grams hydroxyl propyl cellulose. The mixture was blended and placed in a desiccator with an aspirator attached thereto. A portion of the final essentially anhydrous composition was added to water and observed to form a foam as carbon dioxide was released from the carbon dioxide-containing Y zeolite.
Example 4 Example 3 was repeated except that the carbon dioxide-containing zeolite A of example 1 was employed to form an essentially anhydrous composition. The composition was observed to form a foam upon addition to water as carbon dioxide was released from the carbon dioxide-containing zeolite A.
Example 5 Example 4 was repeated except that the peppermint oil was replaced by a sweetner. The toothpaste was observed to foam on being contacted with water as carbon dioxide was released from the carbon dioxide-containing zeolite.
Example 6 The effect temperature on the effervescent activity of the effervescent composition of example 4 was evaluated by evaluating the effervescent time
for three samples (2 grams each) in 500 milliliters of water at 18*C, 32*C and 50*C. The three samples were observed and the time recorded at which effervescent began and ended. The results were as follows:
Water Initial Ending
Temperature Effervescence Effervescence
18°C 35 sec. 7 min. , 53 sec.
32*C 15 sec. 7 min., 30 sec.
50*C 5 sec. 3 min. , 37 sec.
The results indicate that more rapid effervescence occurs at higher temperatures.
Claims
1. An effervescent composition which upon contacting with water provides effervescent and cleaning action comprising an essentially anhydrous base medium and a gas-containing inorganic oxide material containing an effective amount of adsorbed gas to provide effervescence upon contact of the composition with water.
2. The effervescent composition according to claim 1 wherein said gas-containing inorganic oxide material is selected from the group consisting of zeolite A, zeolite B, zeolite X, zeolite Y, zeolite P, zeolite W, zeolite L, zeolite F, ZSM-type zeolites, silicalite, analcite, chabazite, pauligite, ptilolite, ferrierite, mordenite, levynite, clinoptilolite, errionite, aluminophosphates of U.S. Patent No. 4,310,440, silicoaluminophosphates of U.S. Patent No. 4,440,871, aluminas, silicas, silica-aluminas and mixtures thereof.
3. The effervescent compositions according to claim 2, wherein the inorganic oxide material is a zeolite containing cations selected from the group consisting of an alkai metal, alkaline earth metal, zinc, copper and mixtures thereof.
4. The effervescent compositions according to claim 3, wherein the liquid vehicle is an anhydrous humectant or oil selected from the group consisting of glycerine, propylene glycol, polyethylene glycol, mannitol, polypropylene glycol, sorbitol, liquid light petrolatum, mineral oil, vegetable oil, and suitable mixtures thereof.
5. The effervescent composition according to claim 1, which contains an effective amount of a surface-active agent.
6. The effervescent composition according to claim 5 wherein said composition contains between about 0.05 and about 10* by weight of a surface-active agent.
7. The effervescent composition according to claim 5 wherein said surface-active agent is selected from the group consisting of anionic detergents, cationic detergents, nonionic detergents and ampholytic detergents and mixtures thereof.
8. The effervescent composition according to claim 4, which also includes a gelling agent selected from the group consisting of sodium carboxymethyl cellulose, hydroxyethyl cellulose, polyvinyl alcohol, Irish moss, silica aerogel, and mixtures thereof.
9. The effervescent composition according to claim 7, containing 0.5 to 5* of a synthetic anionic surface-active agent.
10. The effervescent composition according to claim 8, which also contains a flavoring agent which is a flavoring oil in an amount of about 0.5 to 2* by weight. - 22 -
11. The effervescent composition according to claim 1, wherein the composition contains an additional abrasive.
12. The effervescent composition according to claim 11, wherein the abrasive is at least one of finely divided silicas, amorphous aluminosilicates and aluminas.
13. The effervescent composition according to claim 1 wherein said effervescent comprises:
(a) between about 5 and about 50 percent by weight of a gas-containing inorganic oxide material selected from the group consisting of zeolite A, zeolite B, zeolite P, zeolite X and mixtures thereof containing between about 1 and about 25 percent by weight of at least one gas selected from the group consisting of nitrogen, oxygen, helium, argon, fluorine, chlorine and carbon dioxide;
(b) at least one liquid vehicle;
(c) at least one surface-active agent; and
(d) at least one gelling agent;
14. The effervescent composition of claim
1 wherein said composition is a powdered composition.
15. An effervescent composition which upon contacting with water provides effervescent and cleaning action comprising an essentially anhydrous base medium and a gas-containing inorganic oxide material containing an effective amount of adsorbed gas to provide effervescence upon contact of the composition with water wherein said inorganic oxide material is selected from the group consisting of the aluminophosphates of U.S. Patent No. 4,310,440, the silicoaluminophosphates of U.S. Patent No. 4,440,871 and mixtures thereof.
16. The effervescent composition of claim 15 wherein the gas is selected from the group consisting of nitrogen, oxygen, helium, argon, fluorine, chlorine, carbon dioxide and mixtures thereof.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE8585906000T DE3578040D1 (en) | 1984-11-16 | 1985-11-15 | BREWING BLENDS. |
| AT85906000T ATE53293T1 (en) | 1984-11-16 | 1985-11-15 | FRESH MIXES. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US672,350 | 1984-11-16 | ||
| US06/672,350 US4592855A (en) | 1984-11-16 | 1984-11-16 | Effervescent compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1986002832A1 true WO1986002832A1 (en) | 1986-05-22 |
Family
ID=24698172
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US1985/002249 Ceased WO1986002832A1 (en) | 1984-11-16 | 1985-11-15 | Effervescent compositions |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4592855A (en) |
| EP (1) | EP0201589B1 (en) |
| JP (1) | JPS62501295A (en) |
| DE (1) | DE3578040D1 (en) |
| WO (1) | WO1986002832A1 (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2597338A1 (en) * | 1986-04-17 | 1987-10-23 | Ruffray Marc | Effervescent foam bath |
| EP0229616A3 (en) * | 1986-01-08 | 1988-11-09 | Kao Corporation | Bath additive composition |
| EP0272878A3 (en) * | 1986-12-16 | 1989-04-12 | Sunstar Kabushiki Kaisha | Dentifrice composition |
| EP0312668A1 (en) * | 1986-04-17 | 1989-04-26 | CHRY Sarl | Effervescent foaming bath product |
| WO1989003670A1 (en) * | 1987-10-22 | 1989-05-05 | Chry Sarl | Effervescent foaming bath |
| WO2001012766A1 (en) * | 1999-08-19 | 2001-02-22 | The Procter & Gamble Company | Method for improving effervescency of a detergent product |
| US6444132B1 (en) * | 1998-04-23 | 2002-09-03 | Tokyo Magnetic Printing Co., Ltd. | Free abrasive slurry compositions |
| US6933266B2 (en) | 2003-05-27 | 2005-08-23 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Effervescent cleaning composition for use in fabric washing |
| WO2005058254A3 (en) * | 2003-12-08 | 2005-08-25 | Unilever Plc | Self foaming non-aqueous personal wash cleansers with little or no surfactant |
| US7012056B2 (en) | 2003-04-17 | 2006-03-14 | Unilever Home & Personal Care Usa | Effervescent cleaning composition comprising surfactant, builder, and dissolved gas |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8421226D0 (en) * | 1984-08-21 | 1984-09-26 | Int Conferences Ab | Tooth cleaning tablet |
| US4839970A (en) * | 1985-07-05 | 1989-06-20 | Siemens Aktiengesellschaft | Filling compound for light waveguide leads and/or light waveguide cables |
| US4824590A (en) * | 1986-09-08 | 1989-04-25 | The Procter & Gamble Company | Thickened aqueous compositions with suspended solids |
| AR244505A1 (en) * | 1988-05-14 | 1993-11-30 | Deutsche Ges Schaedlingsbek | A method for preventing or delaying the formation of undesired phosphine levels in an environment, and the pesticide method for carrying it out. |
| US5817294A (en) * | 1990-11-02 | 1998-10-06 | Arnold; Michael J. | Plaque adsorbent oral composition and method |
| AT404095B (en) * | 1993-12-10 | 1998-08-25 | Petritsch Erich | CLEANING AND CARE PRODUCTS FOR HUMAN HAIR AND METHOD FOR THE PRODUCTION THEREOF |
| US5720949A (en) * | 1996-05-06 | 1998-02-24 | Bristol-Myers Squibb Company | Foamable cosmetic mask product |
| GB2334961A (en) * | 1998-03-03 | 1999-09-08 | Procter & Gamble | Detergent particle |
| GB2334962A (en) * | 1998-03-03 | 1999-09-08 | Procter & Gamble | Foaming component |
| WO1999064556A1 (en) * | 1998-06-05 | 1999-12-16 | The Procter & Gamble Company | Non-aqueous, liquid detergent compositions containing gasified particulate matter |
| US6063390A (en) * | 1998-08-07 | 2000-05-16 | Chesebrough-Pond's Usa Co., A Division Of Conopco, Inc. | Cosmetic effervescent cleansing pillow |
| DE69928011T3 (en) * | 1999-01-12 | 2009-07-09 | Phyzz, Inc., Cincinnati | EXOTHERMIC BRUSH PREPARATION FOR THE IMPROVED DISPERSION OF AROMAS |
| ATE343364T1 (en) * | 1999-06-09 | 2006-11-15 | Wella Ag | USE OF SOLID, GASIFIED PARTICLES FOR HAIR TREATMENTS AND HAIR TREATMENT PRODUCTS CONTAINING SAME |
| DE10019313B4 (en) * | 2000-04-19 | 2004-09-30 | Wella Ag | Instant gel with acoustic indicator, agents containing it, process for its production, and the use of gasified particles as an acoustic indicator |
| US6310014B1 (en) * | 1999-10-05 | 2001-10-30 | Phyzz Inc. | Personal and household care compositions |
| US6451331B1 (en) | 2000-01-31 | 2002-09-17 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Pleated cosmetic effervescent cleansing pillow |
| EP1167501B1 (en) * | 2000-06-19 | 2006-05-24 | The Procter & Gamble Company | Process of treating a fabric by generating heat |
| GB2378716B (en) * | 2001-08-08 | 2004-01-14 | Mi Llc | Process fluid |
| KR101056573B1 (en) * | 2003-12-24 | 2011-08-11 | 주식회사 엘지생활건강 | Non-aqueous Effervescent Toothpaste Composition |
| US20050244212A1 (en) * | 2004-04-30 | 2005-11-03 | Kimberly-Clark Worldwide, Inc. | Foam generating article |
| US7179772B2 (en) * | 2004-06-24 | 2007-02-20 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Extended lathering pillow article for personal care |
| JP2009500490A (en) | 2005-06-29 | 2009-01-08 | ザ プロクター アンド ギャンブル カンパニー | Use of effervescent products for washing dirty dishes by hand washing |
| US7261742B2 (en) | 2005-10-13 | 2007-08-28 | S.C. Johnson & Son, Inc. | Method of deodorizing a textile |
| US7407922B2 (en) * | 2005-10-13 | 2008-08-05 | S.C. Johnson & Son, Inc. | Deodorizing compositions |
| US10624922B2 (en) | 2014-01-31 | 2020-04-21 | Sorption Therapeutics, Llc | Methods and compositions for treating skin |
| DE102014219580A1 (en) | 2014-09-26 | 2016-03-31 | Beiersdorf Ag | Heat-generating anhydrous cleaning preparation |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR891661A (en) * | 1941-10-24 | 1944-03-15 | Process to improve soaps and detergents | |
| US3316691A (en) * | 1966-05-31 | 1967-05-02 | Union Carbide Corp | Fluid encapsulation product |
| FR2283982A1 (en) * | 1974-09-06 | 1976-04-02 | Colgate Palmolive Co | TISSUE SOFTENING COMPOSITION CONTAINING A ZEOLITHIC MOLECULAR SIEVE |
| FR2370710A1 (en) * | 1976-11-15 | 1978-06-09 | Union Carbide Corp | ZEOLITE AGGLOMERS HAVING A REGULATED PORE STRUCTURE, AND THEIR APPLICATION |
| DE3224970A1 (en) * | 1982-07-03 | 1984-01-05 | Fa. J.S. Staedtler, 8500 Nürnberg | A method for cleaning writing, drawing or painting equipment and composition for carrying out the method |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB332142A (en) * | ||||
| US1616202A (en) * | 1923-06-09 | 1927-02-01 | Aquazone Corp | Process of making aqueous solutions and the product |
| US2979157A (en) * | 1942-10-23 | 1961-04-11 | American Viscose Corp | Process for producing gas-proof and gas-adsorbent materials and the articles so produced |
| FR981661A (en) * | 1949-01-07 | 1951-05-29 | Purification Ind Des Gaz Soc D | Method and device for smoking cured meats or the like |
| CA758049A (en) * | 1960-07-19 | 1967-05-02 | The Gillette Company | Heat-generating cosmetic composition |
| US3574824A (en) * | 1968-05-03 | 1971-04-13 | Warner Lambert Pharmaceutical | Anhydrous toothpaste formulation |
| US3639568A (en) * | 1968-09-23 | 1972-02-01 | Alberto Culver Co | Gas-releasable and foamable compositions |
| GB1304090A (en) * | 1970-11-27 | 1973-01-24 | ||
| US3790370A (en) * | 1971-12-23 | 1974-02-05 | Univ Sherbrooke | Removal and recovery of metals from polluted waters |
| IT1031553B (en) * | 1974-02-27 | 1979-05-10 | Rca Corp | DEFLECTION SYSTEM |
| BR7700632A (en) * | 1976-02-05 | 1977-10-04 | Grace W R & Co | PROCESS TO PREPARE ORAL TOOTHPASTE COMPOSITION |
| AT358147B (en) * | 1976-12-03 | 1980-08-25 | Gergely Gerhard | CLEANING MATERIAL |
| US4187287A (en) * | 1977-08-24 | 1980-02-05 | Colgate Palmolive Company | Warm two tone flavored dentifrice |
| US4132771A (en) * | 1977-08-24 | 1979-01-02 | Schreiber Ronald S | Warm two tone flavored dentifrice |
| DE2757280A1 (en) * | 1977-12-22 | 1979-07-05 | Blendax Werke Schneider Co | TOOTHPASTE |
| DE2757290A1 (en) * | 1977-12-22 | 1979-07-05 | Blendax Werke Schneider Co | TOOTHPASTE |
| US4159316A (en) * | 1978-03-06 | 1979-06-26 | Colgate Palmolive Company | Self-heating dentifrice |
| US4349533A (en) * | 1979-08-20 | 1982-09-14 | Pq Corporation | Toothpaste containing pH-adjusted zeolite |
| CA1170187A (en) * | 1980-08-21 | 1984-07-03 | Rimantas Glemza | Synthetic zeolite-containing dentifrice |
| US4578265A (en) * | 1981-08-13 | 1986-03-25 | Laclede Professional Products, Inc. | Di-enzymatic dentifrice |
| GB2109682B (en) * | 1981-11-19 | 1985-09-11 | Colgate Palmolive Co | Stable dentifrice |
-
1984
- 1984-11-16 US US06/672,350 patent/US4592855A/en not_active Expired - Fee Related
-
1985
- 1985-11-15 DE DE8585906000T patent/DE3578040D1/en not_active Expired - Fee Related
- 1985-11-15 EP EP85906000A patent/EP0201589B1/en not_active Expired - Lifetime
- 1985-11-15 JP JP60505258A patent/JPS62501295A/en active Pending
- 1985-11-15 WO PCT/US1985/002249 patent/WO1986002832A1/en not_active Ceased
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR891661A (en) * | 1941-10-24 | 1944-03-15 | Process to improve soaps and detergents | |
| US3316691A (en) * | 1966-05-31 | 1967-05-02 | Union Carbide Corp | Fluid encapsulation product |
| FR2283982A1 (en) * | 1974-09-06 | 1976-04-02 | Colgate Palmolive Co | TISSUE SOFTENING COMPOSITION CONTAINING A ZEOLITHIC MOLECULAR SIEVE |
| FR2370710A1 (en) * | 1976-11-15 | 1978-06-09 | Union Carbide Corp | ZEOLITE AGGLOMERS HAVING A REGULATED PORE STRUCTURE, AND THEIR APPLICATION |
| DE3224970A1 (en) * | 1982-07-03 | 1984-01-05 | Fa. J.S. Staedtler, 8500 Nürnberg | A method for cleaning writing, drawing or painting equipment and composition for carrying out the method |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0229616A3 (en) * | 1986-01-08 | 1988-11-09 | Kao Corporation | Bath additive composition |
| FR2597338A1 (en) * | 1986-04-17 | 1987-10-23 | Ruffray Marc | Effervescent foam bath |
| EP0312668A1 (en) * | 1986-04-17 | 1989-04-26 | CHRY Sarl | Effervescent foaming bath product |
| EP0272878A3 (en) * | 1986-12-16 | 1989-04-12 | Sunstar Kabushiki Kaisha | Dentifrice composition |
| WO1989003670A1 (en) * | 1987-10-22 | 1989-05-05 | Chry Sarl | Effervescent foaming bath |
| US6444132B1 (en) * | 1998-04-23 | 2002-09-03 | Tokyo Magnetic Printing Co., Ltd. | Free abrasive slurry compositions |
| WO2001012766A1 (en) * | 1999-08-19 | 2001-02-22 | The Procter & Gamble Company | Method for improving effervescency of a detergent product |
| US7012056B2 (en) | 2003-04-17 | 2006-03-14 | Unilever Home & Personal Care Usa | Effervescent cleaning composition comprising surfactant, builder, and dissolved gas |
| US6933266B2 (en) | 2003-05-27 | 2005-08-23 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Effervescent cleaning composition for use in fabric washing |
| WO2005058254A3 (en) * | 2003-12-08 | 2005-08-25 | Unilever Plc | Self foaming non-aqueous personal wash cleansers with little or no surfactant |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62501295A (en) | 1987-05-21 |
| DE3578040D1 (en) | 1990-07-12 |
| EP0201589B1 (en) | 1990-06-06 |
| US4592855A (en) | 1986-06-03 |
| EP0201589A1 (en) | 1986-11-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4592855A (en) | Effervescent compositions | |
| US4627972A (en) | Effervescent dentifrice | |
| US4818518A (en) | Effervescent dentifrice | |
| US4132771A (en) | Warm two tone flavored dentifrice | |
| US4187287A (en) | Warm two tone flavored dentifrice | |
| US4071615A (en) | Flavored dentifrice | |
| US3929988A (en) | Flavored dentifrice | |
| US4159316A (en) | Self-heating dentifrice | |
| US3911104A (en) | Gel dentifrices | |
| US3957964A (en) | Dentifrice containing encapsulated flavoring | |
| CA1255605A (en) | Anhydrous dentifrice | |
| US6379652B1 (en) | Oral compositions for reducing mouth odors | |
| US4647451A (en) | Anhydrous dentifrice | |
| US4071614A (en) | Dentifrice containing encapsulated flavoring | |
| US4826676A (en) | Anticariogenic and anticalculus compositions containing zeolitic zinc cations | |
| EA001791B1 (en) | Dentrifice composition | |
| CA1270201A (en) | Stable flavor-containing dentifrice | |
| US4170635A (en) | Flavored dentifrice | |
| EP1257250A2 (en) | System consisting of a dental cleaning agent containing propellant gas and a dispenser | |
| CA1292948C (en) | Effervescent compositions | |
| MX2011004574A (en) | Shelf stable capsules. | |
| AU749805B2 (en) | Dual component dentifrice composition for fluoridating teeth | |
| JPH08169811A (en) | Toothpaste composition | |
| DE10008834A1 (en) | Mousse-forming tooth cleaner, especially toothpaste, contains surfactant, humectant, water and propellant gas, packed in dispenser with mechanically-actuated valve | |
| US6113885A (en) | Polyolefin packaged dentifrice having reduced flavor loss |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AK | Designated states |
Kind code of ref document: A1 Designated state(s): JP |
|
| AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): AT BE CH DE FR GB IT LU NL SE |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 1985906000 Country of ref document: EP |
|
| WWP | Wipo information: published in national office |
Ref document number: 1985906000 Country of ref document: EP |
|
| WWG | Wipo information: grant in national office |
Ref document number: 1985906000 Country of ref document: EP |